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FDA 510(k), K090160, SUPRATHEL WOUND AND BURN DRESSING
FDA 510(k), K090160, SUPRATHEL WOUND AND BURN DRESSING
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510(K) Number: K090160
Device Name: SUPRATHEL WOUND AND BURN DRESSING
Manufacturer: POLYMEDICS INNOVATIONS GMBH
Device Classification Name: absorbable synthetic wound dressing
Regulation Number:
Classification Product Code: QSZ
Date Received: 01/22/2009
Decision Date: 05/20/2009
Regulation Medical Specialty:
Device Name: SUPRATHEL WOUND AND BURN DRESSING
Manufacturer: POLYMEDICS INNOVATIONS GMBH
Device Classification Name: absorbable synthetic wound dressing
Regulation Number:
Classification Product Code: QSZ
Date Received: 01/22/2009
Decision Date: 05/20/2009
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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